Wu Chih-Chan, Okano Kenji, Religia Pijar, Soma Yuki, Takahashi Masatomo, Izumi Yoshihiro, Bamba Takeshi, Honda Kohsuke
International Center for Biotechnology Osaka University Suita Osaka Japan.
Department of Life Science and Biotechnology Faculty of Chemistry Materials and Bioengineering Kansai University Suita Osaka Japan.
Eng Life Sci. 2025 Jan 29;25(1):e70003. doi: 10.1002/elsc.70003. eCollection 2025 Jan.
The oleaginous yeast is recognized for its remarkable lipid accumulation under nitrogen-limited conditions. However, precise control of microbial lipid production in remains challenging due to the complexity of nutrient media. We developed a two-stage fed-batch fermentation process using a well-defined synthetic medium in a 5-L bioreactor. In the first stage, the specific growth rate was maintained at a designated level by maximizing the cell density through optimizing the feeding rate, molar carbon-to-nitrogen (C/N) ratio, and phosphate concentration in feeding media, achieving a high cell density of 213 ± 10 × 10 cells mL. In the second stage, we optimized the molar C/N ratio in the feeding medium for lipid production and achieved high biomass (130 ± 5 g L), lipid titer (88 ± 6 g L), and lipid content (67% ± 2% of dry cellular weight). Our approach yielded a high lipid titer, comparable to the highest reported value of 68 g L achieved in a nutrient medium, by optimizing cultivation conditions with a synthetic medium in . This highlights the importance of well-established yet powerful bioprocess approaches for the precise control of microbial cultivation.
产油酵母因其在氮限制条件下显著的脂质积累而受到认可。然而,由于营养培养基的复杂性,精确控制微生物脂质生产仍然具有挑战性。我们在5升生物反应器中使用明确的合成培养基开发了一种两阶段补料分批发酵工艺。在第一阶段,通过优化补料速率、摩尔碳氮比(C/N)和补料培养基中的磷酸盐浓度来最大化细胞密度,从而将比生长速率维持在指定水平,实现了213±10×10⁶个细胞/毫升的高细胞密度。在第二阶段,我们优化了补料培养基中用于脂质生产的摩尔C/N比,并实现了高生物量(130±5克/升)、脂质滴度(88±6克/升)和脂质含量(占干细胞重量的67%±2%)。我们的方法通过在5升中用合成培养基优化培养条件,获得了高脂质滴度,与在营养培养基中报道的最高值68克/升相当。这突出了成熟且强大的生物工艺方法对于精确控制微生物培养的重要性。